Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9838540
rs9838540
Entrez Id: 131368
Gene Symbol: ZPLD1
ZPLD1
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs9838540
rs9838540
Entrez Id: 131368
Gene Symbol: ZPLD1
ZPLD1
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs1585775
rs1585775
Entrez Id: 131368
Gene Symbol: ZPLD1
ZPLD1
CUI: C3548479
Disease:
response to bronchodilator 		T 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs985375
rs985375
Entrez Id: 131368
Gene Symbol: ZPLD1
ZPLD1
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs17822656
rs17822656
Entrez Id: 131368
Gene Symbol: ZPLD1
ZPLD1
CUI: C3665346
Disease:
Unspecified visual loss 		0.010 GeneticVariation BEFREE In the combined analysis of GWAS and the replication study, no loci reached genome-wide significant level; however, we found four variants showed suggestive level of associations with visual loss at month three (rs17822656, rs76150532, rs17296444, and rs75165563: P<sub>combined</sub> < 1.0 × 10<sup>-5</sup>). 30054556 2018